CN109396427A - A kind of compound dental lamina of base steel and preparation method thereof - Google Patents
A kind of compound dental lamina of base steel and preparation method thereof Download PDFInfo
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- CN109396427A CN109396427A CN201811600241.4A CN201811600241A CN109396427A CN 109396427 A CN109396427 A CN 109396427A CN 201811600241 A CN201811600241 A CN 201811600241A CN 109396427 A CN109396427 A CN 109396427A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
- B22F3/04—Compacting only by applying fluid pressure, e.g. by cold isostatic pressing [CIP]
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/14—Both compacting and sintering simultaneously
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/004—Heat treatment of ferrous alloys containing Cr and Ni
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/0081—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for slabs; for billets
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
- C22C1/058—Mixtures of metal powder with non-metallic powder by reaction sintering (i.e. gasless reaction starting from a mixture of solid metal compounds)
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/005—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides comprising a particular metallic binder
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/12—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on oxides
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C30/00—Alloys containing less than 50% by weight of each constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
- C22C33/0278—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
- C22C33/0285—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5% with Cr, Co, or Ni having a minimum content higher than 5%
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/04—Making ferrous alloys by melting
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/50—Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
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Abstract
The present invention provides a kind of preparation methods of the compound dental lamina of base steel, belong to technical field of composite materials, the type that the present invention passes through control raw material, amount ratio and preparation method, ceramic phase reinforcement obtained includes the iron of ceramic hard phase and non-rigid phase, ceramic hard mutually includes aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide, on the one hand high component (> 50%) is solved, barrier of the ceramic particle Dispersed precipitate of small particle (1000 μm of <) in steel material, on the other hand it solves the problems, such as to wash away containing ceramic phase reinforcement in high-temperature steel iron liquid easily defeated and dispersed, ceramic phase reinforcement is eliminated simultaneously is also easy to produce stomata in later period casting recombination process, slag inclusion, the defects of crackle, the compound dental lamina defect of base steel obtained significantly reduces, improve wear-resisting property.Embodiment statistics indicate that, the compound dental lamina wear-resisting property of base steel provided by the invention is excellent.
Description
Technical field
The present invention relates to technical field of composite materials more particularly to a kind of compound dental lamina of base steel and preparation method thereof.
Background technique
Metal material is most important engineering material, and in metal material, 90% is steel, and steel material has price just
Preferably, it resourceful, superior performance and easy the features such as accomplishing scale production, is widely used.How steel material is improved
Performance also become lot of domestic and foreign scholar research target, one of them important research direction is exactly iron base composite material
Development and application.The reinforcement particle of low-density, high rigidity and high intensity, which is added in steel substrate, prepares particle reinforced iron
Based composites improve its elasticity modulus, hardness, wearability and high-temperature behavior, answer extensively while reducing density of material
For industrial circles such as wear parts.
Hard ceramic micro mist, such as ZrO2、Al2O3, the densification micro mist such as WC, hardness is generally higher than steel material, is ideal
Steel-based composite material enhances particle.Studies have shown that the lesser composite material of particle size yield stress with higher, and
Under the working conditions such as fretting wear, usually the enhancing grain volume fraction of abrasion working face is also required to be greater than 50%, conventional system
Standby technique is difficult to realize.
Scattered plum of Zhao etc., which reports, can prepare 2~3mmZTA ceramic particle enhancing steel-based composite material (referring to " ZTA/
The preparation and polishing machine research of rich chromium cast iron based composites ", Zhao dissipates plum etc., foundry engieering, 2011,32 (12): 1673-
1676), but the ZTA ceramic particle for 50 μm of partial size <, since micro- intergranular pore is too small, storeroom wetability and steel
The limitation of the factors such as mobility, is difficult to prepare using casting infiltration.CN1297798A, which is disclosed, first prepares reinforcement green body, then passes through casting
Sintering technology makes to be pasted onto green compact sintering densification on mould wall simultaneously using casting process high-temperature molten steel or the heat of molten iron
High-temperature chemical reaction occurs, thus the composite surface material layer stable in cast(ing) surface generation surfacing, thickness.Utilize molten iron
Heat in cavity filling process, in-situ preparation VC, TiC etc. in reinforcement are completed at the same time the metallurgical interface knot of reinforcement and matrix
It closes.But this method reinforcement has three: 1) internal-response is violent, and heat, volume fluctuation are huge, reinforcement and base
There is shrinkage cavity, stress collection moderate defect in body interface, and since molten iron casting filling time is short, ferroalloy quick solidification, internal gas
Hole, stress etc. can not be discharged or discharge the short time, will lead to form a large amount of initial crack sources;2) it washes away in high-temperature steel iron liquid and easily bursts
It dissipates;3) in the case where filling time of casting is short, thermal capacity leads to the graphite being added reaction not exclusively, remains stone in cast-internal
Ink dot defect reduces material mechanical performance.
Summary of the invention
In view of this, the purpose of the present invention is to provide compound dental laminas of a kind of base steel and preparation method thereof.The present invention improves
The content of hard phase in reinforcement makes the ceramic particle Dispersed precipitate of small particle (< 1000 μm) in the barrier of steel material, simultaneously
The defects of reinforcement is also easy to produce stomata, slag inclusion, crackle in later period casting recombination process is eliminated, the resistance to of the compound dental lamina of base steel is improved
Grind performance.
In order to achieve the above-mentioned object of the invention, the present invention the following technical schemes are provided:
A kind of preparation method of the compound dental lamina of base steel, comprising the following steps:
(1) raw material is mixed, obtains admixed finepowder, the raw material includes following components in percentage by weight: 10~60%
Hard ceramic powder, 10~22% high-carbon chromium iron, 2~4.5% vanadium iron powder, 1~2.5% carbonized titanium powder, 1.5~
3.5% nickel powder and 25~70% reduced iron powder;
(2) ball milling after mixing the admixed finepowder that the step (1) obtains with dehydrated alcohol, obtains ball milling product;
(3) isostatic pressing is carried out after drying the ball milling product that the step (2) obtains, obtains ceramic phase reinforcement base
Body;
(4) the ceramic phase reinforcement green body hot pressed sintering for obtaining the step (3), obtains ceramic phase reinforcement;
(5) casting steel melt, obtains base steel after the ceramic phase reinforcement that the step (4) obtains being fixed in dental lamina sand mold
Compound dental lamina idiosome;
(6) the compound dental lamina idiosome of base steel that the step (5) obtains is heat-treated, obtains the compound dental lamina of base steel.
Preferably, in the step (1) average grain diameter of hard ceramic powder less than 1000 μm.
Preferably, hard ceramic powder includes Al in the step (1)2O3·ZrO2Complex-phase ceramic micropowder and/or ZrO2It is micro-
Powder.
Preferably, the pressure of isostatic pressing is 180~300MPa, the guarantor of the isostatic pressing in the step (3)
The pressure time is 0.5~1h.
Preferably, the temperature of hot pressed sintering is 1230~1550 DEG C in the step (4), and the pressure of the hot pressed sintering is
20~50MPa, the time of the hot pressed sintering are 0.5~2h.
Preferably, the time of ball milling is 12~36h in the step (2), and the revolving speed of the ball milling is 100~300rpm.
Preferably, temperature dry in the step (3) is 100~250 DEG C, and the time of the drying is 2~5h.
Preferably, the temperature cast in the step (4) is 1400~1600 DEG C.
Preferably, the temperature being heat-treated in the step (6) is 1020~1070 DEG C, and the time is 1~2h.
The present invention also provides the compound dental laminas of base steel made from preparation method described in above-mentioned technical proposal.
The present invention provides a kind of preparation methods of the compound dental lamina of base steel, and raw material is mixed, and obtain admixed finepowder, the original
Material includes following components in percentage by weight: 10~60% hard ceramic powder, 10~22% high-carbon chromium iron, 2~4.5%
Vanadium iron powder, 1~2.5% carbonized titanium powder, 1.5~3.5% nickel powder and 25~70% reduced iron powder;By admixed finepowder
Ball milling after mixing with dehydrated alcohol obtains ball milling product;Isostatic pressing will be carried out after the drying of ball milling product, obtains ceramic enhancing
Body green body;By ceramic phase reinforcement green body hot pressed sintering, ceramic phase reinforcement is obtained;After ceramic phase reinforcement is fixed in dental lamina sand mold
Casting steel melt, obtains the compound dental lamina idiosome of base steel;The compound dental lamina idiosome of base steel is heat-treated, the compound tooth of base steel is obtained
Plate.The present invention is compared with casting-sinter process, by hot-pressing sintering technique, makes VC, Cr in ceramic phase reinforcement7C3Etc. reinforced phases conjunction
Occur in this process procedure at reaction, makes heat absorption, the heat release of material, contraction, expansion of volume etc. occur in advance, keep away in this way
Exempt from the short time in casting process physical chemistry transformation, cause composite material remaining pore defect, interface residual stress it is excessive,
The problems such as reaction is not exclusively, product property is undesirable;Compared with gravity or pressure casting infiltration, ceramic phase reinforcement hole obtained is equal
Even, steel melt can preferably penetrate into;Compared with stirring-centre spinning, ceramic particle agglomeration is avoided, and ceramics are micro-
Uniform particle sizes' distribution of grain, is conducive to industry application;The present invention is low in cost simultaneously, can mechanization degree it is high, adapt to advise greatly
Mould production, promotion prospect are very wide.Type, amount ratio and preparation method of the present invention by control raw material, pottery obtained
Porcelain reinforcement includes the iron of ceramic hard phase and non-rigid phase, and ceramic hard mutually includes aluminium oxide, zirconium oxide, vanadium carbide, carbonization
On the one hand titanium and chromium carbide solve the ceramic particle Dispersed precipitate of high component (> 50%), small particle (1000 μm of <) in steel
The barrier of iron material, on the other hand solves the problems, such as to wash away containing ceramic phase reinforcement in high-temperature steel iron liquid easy to be defeated and dispersed, while eliminating pottery
The defects of porcelain reinforcement is also easy to produce stomata, slag inclusion, crackle in later period casting recombination process, the compound dental lamina defect of base steel obtained
It significantly reduces, improves wear-resisting property.Embodiment statistics indicate that, the compound dental lamina of base steel provided by the invention than steel matrix be made
The wear-resisting property of dental lamina improve 1.5~2 times.
Specific embodiment
The present invention provides a kind of preparation methods of the compound dental lamina of base steel, comprising the following steps:
(1) raw material is mixed, obtains admixed finepowder, the raw material includes following components in percentage by weight: 10~60%
Hard ceramic powder, 10~22% high-carbon chromium iron, 2~4.5% vanadium iron powder, 1~2.5% carbonized titanium powder, 1.5~
3.5% nickel powder and 25~70% reduced iron powder;
(2) ball milling after mixing the admixed finepowder that the step (1) obtains with dehydrated alcohol, obtains ball milling product;
(3) isostatic pressing is carried out after drying the ball milling product that the step (2) obtains, obtains ceramic phase reinforcement base
Body;
(4) the ceramic phase reinforcement green body hot pressed sintering for obtaining the step (3), obtains ceramic phase reinforcement;
(5) casting steel melt, obtains base steel after the ceramic phase reinforcement that the step (4) obtains being fixed in dental lamina sand mold
Compound dental lamina idiosome;
(6) the compound dental lamina idiosome of base steel that the step (5) obtains is heat-treated, obtains the compound dental lamina of base steel.
The present invention mixes raw material, obtains admixed finepowder, and the raw material includes following components in percentage by weight: 10~
60% hard ceramic powder, 10~22% high-carbon chromium iron, 2~4.5% vanadium iron powder, 1~2.5% carbonized titanium powder, 1.5
~3.5% nickel powder and 25~70% reduced iron powder.
In the present invention, the weight percent of hard ceramic powder is preferably 45% in the raw material.In the present invention, described
The average grain diameter of hard ceramic powder is preferably smaller than 1000 μm, more preferably less than 900 μm.
In the present invention, the hard ceramic powder preferably includes Al2O3·ZrO2Complex-phase ceramic micropowder and/or ZrO2Micro mist.
The present invention is to the Al2O3·ZrO2Complex-phase ceramic micropowder and ZrO2The source of micro mist does not have special restriction, using this field skill
Commercial goods known to art personnel.
In the present invention, the weight percent of the raw material medium high carbon ferrochrome powder is preferably 17.6%.In the present invention, institute
State the component that high-carbon chromium iron preferably comprises following mass fraction: C 6.0~10.0%, Cr62~72%, Fe 20~35%.
The present invention does not have special restriction to the source of the high-carbon chromium iron, is using commercial goods well known to those skilled in the art
It can.
In the present invention, the weight percent of vanadium iron powder is preferably 3.6% in the raw material.In the present invention, the vanadium
Iron powder preferably comprises the component of following mass fraction: V 35~65%, Fe 35~65%.The present invention carrys out the vanadium iron powder
Source does not have special restriction, using commercial goods well known to those skilled in the art.
In the present invention, the weight percent of carbonized titanium powder is preferably 1.8% in the raw material.The present invention is to the carbonization
The source of titanium valve does not have special restriction, using commercial goods well known to those skilled in the art.
In the present invention, the weight percent of nickel powder is preferably 2% in the raw material.Source of the present invention to the nickel powder
There is no special restriction, using commercial goods well known to those skilled in the art.
In the present invention, the weight percent of reduced iron powder is preferably 30% in the raw material.The present invention is to the reduction
The source of iron powder does not have special restriction, using commercial goods well known to those skilled in the art.
After obtaining admixed finepowder, ball milling after the present invention mixes the admixed finepowder with dehydrated alcohol obtains ball milling product.
In the present invention, the time of the ball milling is preferably 12~36h, and the revolving speed of the ball milling is preferably 100~300rpm.
In the present invention, the amount ratio of the admixed finepowder and dehydrated alcohol is preferably 100g:40~60mL.
After obtaining ball milling product, the present invention will carry out isostatic pressing after ball milling product drying, obtain ceramic enhancing
Body green body.In the present invention, the temperature of the drying is preferably 100~250 DEG C, and more preferably 150 DEG C, the time of the drying
Preferably 2~5h, more preferably 3h.In the present invention, the drying preferably carries out in a vacuum drying oven.
In the present invention, the pressure of the isostatic pressing is preferably 180~300MPa, more preferably 250MPa, described
The dwell time of isostatic pressing is preferably 0.5~1h.
After obtaining ceramic phase reinforcement green body, the ceramic phase reinforcement green body hot pressed sintering is obtained ceramic enhancing by the present invention
Body.
In the present invention, the temperature of the hot pressed sintering is preferably 1230~1550 DEG C, and more preferably 1250 DEG C, the heat
The pressure of pressure sintering is preferably 20~50MPa, and more preferably 30MPa, the time of the hot pressed sintering is preferably 0.5~2h, more
Preferably 1h.The present invention makes VC, Cr in ceramic phase reinforcement by hot-pressing sintering technique7C3Etc. reinforced phases synthetic reaction at this
Occur in process procedure, make heat absorption, the heat release of material, contraction, expansion of volume etc. occur in advance, thus be avoided that in casting process
The physical chemistry of middle short time changes, cause composite material remaining pore defect, interface residual stress is excessive, reaction is incomplete,
The problems such as product property is undesirable.
In the present invention, ceramic phase reinforcement includes the iron of ceramic hard phase and non-rigid phase.In the present invention, the ceramics are hard
Matter mutually preferably comprises aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide.In the present invention, the shape of the ceramic phase reinforcement
Shape preferably needs compound Region Matching, more preferably strip, bulk or cellular with component.In the present invention, the ceramics increase
The thickness of strong body is preferably 3~80mm.
After obtaining the ceramic phase reinforcement, the present invention pours cast steel after the ceramic phase reinforcement is fixed in dental lamina sand mold and melts
Body obtains the compound dental lamina idiosome of base steel.The present invention does not have special restriction to the dental lamina sand mold or preparation method, using ability
Dental lamina sand mold made from preparation method known to field technique personnel.
In the present invention, the temperature of the casting is preferably 1400~1600 DEG C, more preferably 1420~1580 DEG C, more excellent
It is selected as 1450 DEG C.
In the present invention, the steel melt is preferred from steel alloy or potassium steel.The present invention is to the steel alloy and Gao Meng
The specific ingredient of steel does not have special restriction.
After obtaining the compound dental lamina idiosome of base steel, the compound dental lamina idiosome of the base steel is heat-treated by the present invention, obtains steel
The compound dental lamina of base.
In the present invention, the temperature of the heat treatment is preferably 1020~1070 DEG C, and more preferably 1040~1060 DEG C, when
Between preferably 1~2h, more preferably 1~1.5h.
The present invention also provides the compound dental laminas of base steel made from preparation method described in above-mentioned technical proposal.This hair passes through ceramics
Reinforcement prepares the compound dental lamina of base steel, includes the iron of ceramic hard phase and non-rigid phase in ceramic phase reinforcement, and ceramic hard is mutually excellent
Choosing includes aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide.The present invention by the control type of raw material, amount ratio and
Preparation method, ceramic phase reinforcement obtained include the iron of ceramic hard phase and non-rigid phase, and ceramic hard mutually includes aluminium oxide, oxygen
Change zirconium, vanadium carbide, titanium carbide and chromium carbide, on the one hand solves the ceramics of high component (> 50%), small particle (1000 μm of <)
On the other hand particle Dispersed precipitate solves to wash away containing ceramic phase reinforcement in high-temperature steel iron liquid easily defeated and dispersed in the barrier of steel material
Problem, while the defects of ceramic phase reinforcement is also easy to produce stomata, slag inclusion, crackle in later period casting recombination process is eliminated, it is obtained
The compound dental lamina defect of base steel significantly reduces, and improves wear-resisting property.
Compound dental lamina of base steel provided by the invention and preparation method thereof is described in detail below with reference to embodiment, but
It is that they cannot be interpreted as limiting the scope of the present invention.
The average grain diameter of hard ceramic powder is less than 1000 μm in all embodiments of the invention, high-carbon chromium iron preferably comprise with
The component of lower mass fraction: C 6.0%, Cr 64%, Fe 30%, vanadium iron powder include the component of following mass fraction: V 35%,
Fe 65%.
Embodiment 1
1) raw material and proportion;
Each raw material proportioning of ceramic phase reinforcement is as shown in table 1.
Each raw material proportioning of 1 ceramic phase reinforcement of table
2) above-mentioned admixed finepowder is put into ball grinder, the ratio that the dehydrated alcohol of 40mL is added according to every 100g micro mist is mixed
It closes, drum's speed of rotation 300r/min, mixing time 12h;
3) admixed finepowder by above-mentioned after ball-milling treatment is put into vacuum oven dry, and temperature is 100 DEG C, when dry
Between 5h;
4) above-mentioned admixed finepowder is put into mold and carries out isostatic pressing, pressure 180MP, pressure maintaining 1h;
5) ceramic phase reinforcement green body obtained above is subjected to hot pressed sintering, sintering temperature is 1230 DEG C, and pressure is
50MPa, dwell time 2h keep the temperature 2h;
6) ceramic enhancement phase in ceramic phase reinforcement includes aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide, is increased
Strong body thickness 40mm;
7) dental lamina sand mold is made, ceramic phase reinforcement obtained above is cut into Φ 20 × 30mm size, is placed in sand mold,
Mould assembling;The molten alloy steel in medium-frequency induction furnace, alloy composition C:0.25%, Cr:1.5%, Si:0.5%, Mn:
0.5%, P:0.05%, S:0.0.5%, surplus Fe;Molten steel is poured into, cast temperature is 1580 DEG C, and after cooling, it is multiple to obtain base steel
Close dental lamina idiosome;
8) the compound dental lamina idiosome of the base steel is subjected at 1020 DEG C heat treatment 2h, obtains the compound dental lamina of base steel.
There is original Al in the reinforcement of the compound dental lamina of the base steel2O3·ZrO2Complex phase ceramic and newly-generated TiC, VC,
(Fe、Cr)7C3Etc. a variety of hard reinforced phases, and interface cohesion is good.
The compound dental lamina defect of base steel made from the present embodiment significantly reduces, to the compound dental lamina of base steel made from the present embodiment into
Row wear-resisting property test, as a result, it has been found that the compound dental lamina of base steel made from the present embodiment improves 1.5 than dental lamina made from steel matrix
Times.
Embodiment 2
1) raw material and proportion;
Each raw material proportioning of ceramic phase reinforcement is as shown in table 2.
Each raw material proportioning of 2 ceramic phase reinforcement of table
2) above-mentioned admixed finepowder is put into ball grinder, mixes according to the ratio that the dehydrated alcohol of 60mL is added in every 100g micro mist,
Drum's speed of rotation 100r/min, mixing time 36h;
3) above-mentioned admixed finepowder is put into drying in vacuum oven, temperature is 250 DEG C, drying time 2h;
4) admixed finepowder by above-mentioned after ball-milling treatment is put into mold and carries out isostatic pressing, pressure 300MP, pressure maintaining
0.5h;
5) ceramic phase reinforcement green body obtained above is subjected to hot pressed sintering, sintering temperature is 1230 DEG C, and pressure is
20MPa, dwell time 0.5h keep the temperature 0.5h;
6) ceramic enhancement phase in ceramic phase reinforcement includes aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide etc.,
Enhance body thickness 60mm;
7) dental lamina sand mold is made, ceramic phase reinforcement obtained above is cut into Φ 20 × 30mm size, is placed in sand mold,
Mould assembling;The melting potassium steel in medium-frequency induction furnace, potassium steel ingredient C:1.3%, Cr:2.5%, Si:0.5%, Mn:
14.5%, P:0.05%, S:0.0.5%, surplus Fe;Molten steel is poured into, cast temperature is 1420 DEG C, after cooling, obtains base steel
Compound dental lamina idiosome;
8) the compound dental lamina idiosome of the base steel is subjected at 1070 DEG C heat treatment 1h, obtains the compound dental lamina of base steel.
There is original ZrO in the reinforcement of the compound dental lamina of the base steel2Complex phase ceramic and newly-generated TiC, VC, (Fe, Cr)7C3Etc. a variety of hard reinforced phases, and interface cohesion is good.
The compound dental lamina defect of base steel made from the present embodiment significantly reduces, to the compound dental lamina of base steel made from the present embodiment into
Row wear-resisting property test, as a result, it has been found that the compound dental lamina of base steel made from the present embodiment improves 2 times than dental lamina made from steel matrix.
Embodiment 3
1) raw material and proportion;
Each raw material proportioning of ceramic phase reinforcement is as shown in table 3.
Each raw material proportioning of 3 ceramic phase reinforcement of table
2) above-mentioned admixed finepowder is put into ball grinder, the ratio that the dehydrated alcohol of 40mL is added according to every 100g micro mist is mixed
It closes, drum's speed of rotation 300r/min, mixing time 12h;
3) admixed finepowder by above-mentioned after ball-milling treatment is put into vacuum oven dry, and temperature is 150 DEG C, when dry
Between 5h;
4) above-mentioned admixed finepowder is put into mold and carries out isostatic pressing, pressure 250MP, pressure maintaining 1h;
5) ceramic phase reinforcement green body obtained above is subjected to hot pressed sintering, sintering temperature is 1250 DEG C, and pressure is
30MPa, dwell time 1h keep the temperature 1h;
6) ceramic enhancement phase in ceramic phase reinforcement includes aluminium oxide, zirconium oxide, vanadium carbide, titanium carbide and chromium carbide etc.,
Enhance body thickness 50mm;
7) dental lamina sand mold is made, ceramic phase reinforcement obtained above is cut into Φ 20 × 30mm size, is placed in sand mold,
Mould assembling;The molten alloy steel in medium-frequency induction furnace, alloy composition C:1.35%, Cr:2.5%, Si:0.5%, Mn:
17.5%, P:0.05%, S:0.0.5%, surplus Fe;Molten steel is poured into, cast temperature is 1450 DEG C, after cooling, obtains base steel
Compound dental lamina idiosome;
8) the compound dental lamina idiosome of the base steel is subjected at 1050 DEG C heat treatment 1.5h, obtains the compound dental lamina of base steel.
There is original Al in the reinforcement of the compound dental lamina of the base steel2O3·ZrO2Complex phase ceramic and newly-generated TiC, VC,
(Fe、Cr)7C3Etc. a variety of hard reinforced phases, and interface cohesion is good.
The compound dental lamina defect of base steel made from the present embodiment significantly reduces, to the compound dental lamina of base steel made from the present embodiment into
Row wear-resisting property test, as a result, it has been found that the compound dental lamina of base steel made from the present embodiment improves 1.9 than dental lamina made from steel matrix
Times.
The above is only a preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art
For member, various improvements and modifications may be made without departing from the principle of the present invention, these improvements and modifications are also answered
It is considered as protection scope of the present invention.
Claims (10)
1. a kind of preparation method of the compound dental lamina of base steel, which comprises the following steps:
(1) raw material is mixed, obtains admixed finepowder, the raw material includes following components in percentage by weight: 10~60% it is hard
Matter ceramic powder, 10~22% high-carbon chromium iron, 2~4.5% vanadium iron powder, 1~2.5% carbonized titanium powder, 1.5~3.5%
Nickel powder and 25~70% reduced iron powder;
(2) ball milling after mixing the admixed finepowder that the step (1) obtains with dehydrated alcohol, obtains ball milling product;
(3) isostatic pressing is carried out after drying the ball milling product that the step (2) obtains, obtains ceramic phase reinforcement green body;
(4) the ceramic phase reinforcement green body hot pressed sintering for obtaining the step (3), obtains ceramic phase reinforcement;
(5) casting steel melt, it is compound to obtain base steel after the ceramic phase reinforcement that the step (4) obtains being fixed in dental lamina sand mold
Dental lamina idiosome;
(6) the compound dental lamina idiosome of base steel that the step (5) obtains is heat-treated, obtains the compound dental lamina of base steel.
2. preparation method according to claim 1, which is characterized in that the average grain of hard ceramic powder in the step (1)
Diameter is less than 1000 μm.
3. preparation method according to claim 1 or 2, which is characterized in that hard ceramic powder includes in the step (1)
Al2O3·ZrO2Complex-phase ceramic micropowder and/or ZrO2Micro mist.
4. preparation method according to claim 1, which is characterized in that the pressure of isostatic pressing is in the step (3)
180~300MPa, the dwell time of the isostatic pressing are 0.5~1h.
5. preparation method according to claim 1, which is characterized in that the temperature of hot pressed sintering is in the step (4)
1230~1550 DEG C, the pressure of the hot pressed sintering is 20~50MPa, and the time of the hot pressed sintering is 0.5~2h.
6. preparation method according to claim 1, which is characterized in that in the step (2) time of ball milling be 12~
36h, the revolving speed of the ball milling are 100~300rpm.
7. preparation method according to claim 1, which is characterized in that in the step (3) dry temperature be 100~
250 DEG C, the time of the drying is 2~5h.
8. preparation method according to claim 1, which is characterized in that the temperature cast in the step (4) is 1400~
1600℃。
9. preparation method according to claim 1, which is characterized in that the temperature being heat-treated in the step (6) is 1020
~1070 DEG C, the time is 1~2h.
10. the compound dental lamina of base steel made from preparation method described in claim 1~9 any one.
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